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Serum Glycans as Risk Markers for Non-Small Cell Lung Cancer

机译:血清聚糖是非小细胞肺癌的危险标志物

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摘要

Previous studies have suggested occurrence of altered serum glycan profiles in patients with lung cancer. Here, we aimed to determine the predictive value of serum glycans to distinguish non-small cell lung cancer (NSCLC) cases from controls in prediagnostic samples using a previously validated predictive protein marker pro-SFTPB, as anchor. Blinded prediagnostic senim samples were obtained from the Carotene and Retinol Efficacy Mal (CARET), and included a discovery set of 100 NSCLC cases and 199 healthy controls. A second test set consisted of 108 cases and 216 controls. Cases and controls were matched for age at baseline (5-year groups), sex, smoking status (current vs. former), study enrollment cohort, and date of blood draw. Serum glycan profiles were determined by mass spectrometry. Twelve glycan variables were identified to have significant discriminatory power between cases and controls in the discovery set (AUC > 0.6). Of these, four were confirmed in the independent validation set. A combination marker yielded AUCs of 0.74 and 0.64 in the discovery and test set, respectively. Four glycan variables exhibited significant incremental value when combined with pro-SFEPB compared with pro-SFTPB alone with AUCs of 0.73, 0.72, 0.72, and 0.72 in the test set, indicating that serum glycan signatures have relevance to risk assessment for NSCLC. (C) 2016 AACR
机译:先前的研究表明,肺癌患者血清聚糖谱发生改变。在这里,我们旨在确定血清聚糖的预测价值,以使用先前验证的预测蛋白标记物pro-SFTPB作为锚点,将非小细胞肺癌(NSCLC)病例与诊断前样品中的对照区分开。从胡萝卜素和视黄醇功效药物(CARET)中获得了盲诊断的senim样本,包括100例NSCLC病例和199例健康对照的发现。第二个测试集由108个案例和216个对照组组成。病例和对照的基线年龄(5岁组),性别,吸烟状况(当前与以前),研究入组队列和抽血日期相匹配。通过质谱确定血清聚糖谱。鉴定出十二个聚糖变量在发现集的病例和对照之间具有明显的区分能力(AUC> 0.6)。其中,在独立的验证集中确认了四个。在发现和测试集中,组合标记分别产生0.74和0.64的AUC。与单独的pro-SFTPB相比,与单独的SFTPB相比,四个聚糖变量显示出显着的增量值,测试集中的AUC分别为0.73、0.72、0.72和0.72,这表明血清聚糖特征与NSCLC的风险评估相关。 (C)2016年美国癌症研究协会

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